Juvenile myoclonic epilepsy mimic associated with CHD2 gene mutation

This paper reports the electroclinical manifestations of an epilepsy syndrome associated with a chromodomain helicase DNA-binding protein 2 (CHD2) gene mutation with clinical semiology and electroencephalographic (EEG) features consistent with juvenile myoclonic epilepsy (JME). Myoclonic and myoclon...

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Detalles Bibliográficos
Autores principales: Singh, Neeraj, Ritaccio, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6976925/
https://www.ncbi.nlm.nih.gov/pubmed/31993582
http://dx.doi.org/10.1016/j.ebr.2019.100355

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6976925/
https://www.ncbi.nlm.nih.gov/pubmed/31993582
http://dx.doi.org/10.1016/j.ebr.2019.100355

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